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J Bronwyn Bateman Selected Research

Autosomal Dominant Cataract

4/2008Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA).
3/2007Gene conversion mutation in crystallin, beta-B2 (CRYBB2) in a Chilean family with autosomal dominant cataract.
4/2006Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract.

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J Bronwyn Bateman Research Topics

Disease

4Cataract (Cataracts)
04/2008 - 04/2006
3Autosomal Dominant Cataract
04/2008 - 04/2006
1Duane Retraction Syndrome (Duane Syndrome)
03/2009
1Craniopharyngioma (Craniopharyngiomas)
03/2009
1Hyperpigmentation
03/2009
1Epiretinal Membrane (Epiretinal Membranes)
03/2009
1Hearing Loss (Hearing Impairment)
03/2009
1Lissencephaly
03/2009
1Corneal Opacity
04/2008

Drug/Important Bio-Agent (IBA)

2Genetic Markers (Genetic Marker)IBA
04/2008 - 03/2007
2Proteins (Proteins, Gene)FDA Link
08/2007 - 04/2006
1Retinal Pigments (Pigments, Visual)IBA
03/2009
1alpha-Crystallin A ChainIBA
04/2008
1Malondialdehyde (Propanedial)IBA
08/2007
1Crystallins (Crystallin)IBA
03/2007

Therapy/Procedure

1Telescopes
03/2009